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FDA 510(k)

RITTER STERILIZER

K-Number: K801309 · 1980-06-20

ApplicantSybron Corp.
Decision Date1980-06-20
Product CodeFLE
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

RITTER STERILIZER is the device name listed in this FDA 510(k) record. The listed applicant is Sybron Corp.. It received FDA 510(k) clearance on 1980-06-20 under 510(k) number K801309. The device is classified under product code FLE. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RITTER STERILIZER?

RITTER STERILIZER is a medical device that received FDA 510(k) clearance on 1980-06-20. The listed applicant is Sybron Corp.. The 510(k) number is K801309.

When did RITTER STERILIZER receive FDA 510(k) clearance?

RITTER STERILIZER received FDA 510(k) clearance on 1980-06-20, under 510(k) number K801309.

Who is the listed applicant for RITTER STERILIZER?

The FDA 510(k) record lists Sybron Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RITTER STERILIZER?

The FDA product code for RITTER STERILIZER is FLE.

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Related Devices (Code: FLE)

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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